Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs1401496725
REG1A
0.925 0.120 2 79121657 missense variant C/G;T snv 8.0E-06; 8.0E-06 2
rs544706237
REG1A
0.851 0.120 2 79121649 missense variant A/G;T snv 8.0E-06; 5.2E-05 5
rs1205185774
AHSA1
0.882 0.120 14 77469161 missense variant C/T snv 4
rs63750083
PSEN1
0.732 0.160 14 73219177 missense variant C/A;T snv 13
rs63751223
PSEN1
0.807 0.160 14 73219161 missense variant G/C snv 6
rs661
PSEN1
0.807 0.120 14 73217225 missense variant G/A;T snv 4.0E-06 6
rs1566650594
PSEN1
0.851 0.120 14 73206384 splice acceptor variant A/T snv 4
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs63750900
PSEN1
0.763 0.160 14 73198067 missense variant G/A snv 4.0E-06 7.0E-06 9
rs63750526
PSEN1
0.776 0.160 14 73192832 missense variant C/A snv 10
rs63751287
PSEN1
0.742 0.120 14 73192792 missense variant A/G;T snv 13
rs63749836
PSEN1
0.827 0.160 14 73192786 missense variant G/A snv 5
rs63750487
PSEN1
0.882 0.120 14 73192771 missense variant C/T snv 3
rs63750053
PSEN1
0.827 0.120 14 73192721 missense variant G/T snv 5
rs63750082
PSEN1
0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 13
rs63751068
PSEN1
0.827 0.120 14 73186920 missense variant G/C;T snv 6
rs63750590
PSEN1
0.790 0.120 14 73186860 missense variant A/G snv 10
rs63750306
PSEN1
0.701 0.320 14 73173663 missense variant A/C;G;T snv 17
rs63751278
PSEN1
0.827 0.120 14 73173631 missense variant A/G snv 6
rs63750450
PSEN1
0.851 0.120 14 73173571 missense variant A/G snv 4
rs63749824
PSEN1
0.776 0.120 14 73170945 missense variant C/G;T snv 4.0E-06; 1.2E-05 8
rs767076633
TBK1
0.925 0.120 12 64484311 missense variant T/C snv 1.2E-05 2
rs387906711
UBQLN2
0.807 0.120 X 56565389 missense variant C/A;T snv 6.6E-06 6
rs387906709
UBQLN2
0.776 0.120 X 56565363 missense variant C/A;T snv 9